A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696105



Internal ID15086071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:7777235..8379574hg38UCSC Ensembl
InnerchrX:7745276..8347615hg19UCSC Ensembl
InnerchrX:7705276..8307615hg18UCSC Ensembl
InnerchrX:7555012..8157351hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38602340
hg19602340
hg18602340
hg17602340
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518656
Supporting Variants
Samples
Known GenesMIR651, PNPLA4, VCX, VCX2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696105
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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